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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 14 November 2016
Main ID:  NCT02640274
Date of registration: 22/12/2015
Prospective Registration: No
Primary sponsor: Central Norway Regional Health Authority
Public title: Individual Nurse-led Counselling Programme for Patients Early Discharged After Myocardial Infarction.
Scientific title: Self-management Behaviour After an Individual Nurse-led Counselling Programme for Patients Early Discharged After Myocardial Infarction: A Randomised Controlled Trial.
Date of first enrolment: November 2013
Target sample size: 71
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT02640274
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention  
Phase:  N/A
Countries of recruitment
Norway
Contacts
Name:     Liv Heidi Skotnes, phd
Address: 
Telephone:
Email:
Affiliation:  Leangen Hospital HNT
Key inclusion & exclusion criteria

Inclusion Criteria:Patients with documented evidence of myocardial infarction during
hospitalisation will be considered for inclusion.

- patients over 18 years old

- living at home in the local hospital area after hospital discharge

- able to receive telephone calls, fill in questionnaire and communicate in Norwegian.

Exclusion Criteria:

- cognitive impaired/dementia

- planning for coronary artery bypass graft surgery



Age minimum: 18 Years
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Coronary Disease
Cardiovascular Diseases
Myocardial Infarction
Intervention(s)
Behavioral: Nurse-led counselling programme
Other: Usual care
Primary Outcome(s)
Changes in self-management [Time Frame: from baseline to 6 and 12 months of follow-up]
Secondary Outcome(s)
changes in health behaviour [Time Frame: from baseline to 6 and 12 months of follow-up]
Secondary ID(s)
2013/1568/REK
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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